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树突状细胞及其在动脉粥样形成中的作用。

Dendritic cells and their role in atherogenesis.

机构信息

Faculty of Medicine, SOMS, University of New South Wales, Kensington, NSW, Australia.

出版信息

Lab Invest. 2010 Jul;90(7):970-84. doi: 10.1038/labinvest.2010.94. Epub 2010 May 10.

Abstract

Dendritic cells (DCs) are the most potent professional antigen-presenting cells with the unique ability of primary immune response initiation. DCs originate from bone marrow progenitors, which circulate in the peripheral blood and subsequently penetrate peripheral tissues, where they give rise to immature DCs. In peripheral tissues, DCs continuously monitor the microenvironment and, when the cells encounter 'danger' signals, DCs undergo differentiation and maturation. Maturing DCs usually migrate to lymphatic tissues, where they form contacts with T cells to initiate a primary immune response. DCs were identified in arteries in 1995 and since then, further knowledge has been gained about the peculiarities of vascular-associated DCs and their role in atherosclerosis. Immune reactions toward modified lipoproteins and other factors ignited by resident vascular DCs as well as by newly arrived DCs, which originate from blood monocytes, are believed to destabilize arterial homeostasis from very earlier stages of atherogenesis. There is a remarkable heterogeneity of DCs in atherosclerotic lesions. Some DCs mature and become capable of forming clusters with T cells directly within the arterial wall. The predictive value of the numbers of circulating DC precursors in coronary artery disease and in atherosclerosis has been assessed, and it has been shown that DCs have a role in plaque destabilization. Over recent decades, DCs have proven to be a valuable instrument in immunotherapy approaches against cancer and various autoimmune diseases, and this explains the demand that the accumulated knowledge be applied to the field of atherosclerosis immunotherapy.

摘要

树突状细胞(DCs)是最有效的专业抗原呈递细胞,具有启动初级免疫应答的独特能力。DC 起源于骨髓前体,它们在周围血液中循环,随后渗透到外周组织中,在那里它们产生未成熟的 DC。在外周组织中,DC 持续监测微环境,当细胞遇到“危险”信号时,DC 会发生分化和成熟。成熟的 DC 通常迁移到淋巴组织,在那里它们与 T 细胞形成接触,启动初级免疫应答。1995 年在动脉中发现了 DC,从那时起,人们对血管相关 DC 的特性及其在动脉粥样硬化中的作用有了更多的了解。被修饰的脂蛋白和其他由驻留的血管 DC 以及源自血液单核细胞的新到达的 DC 引发的免疫反应被认为会破坏动脉粥样硬化发生的早期阶段的动脉内稳态。动脉粥样硬化病变中的 DC 具有显著的异质性。一些 DC 成熟并能够直接在动脉壁内与 T 细胞形成簇。已经评估了循环 DC 前体数量在冠状动脉疾病和动脉粥样硬化中的预测价值,并且已经表明 DC 在斑块不稳定中起作用。在过去的几十年中,DC 已被证明是癌症和各种自身免疫性疾病免疫治疗方法的有价值工具,这解释了对动脉粥样硬化免疫治疗领域应用积累的知识的需求。

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